Publication:
Critical examination of chemically modified hybrid thermosets: Synthesis, characterization and mechanical behavior in the plateau regime of polyaminosiloxane-nitrile-DGEBA

Loading...
Thumbnail Image
Identifiers
Publication date
2015-07-09
Defense date
Advisors
Tutors
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Impact
Google Scholar
Export
Research Projects
Organizational Units
Journal Issue
Abstract
Poly(3-aminopropylmethylsiloxane) has been modified with acrylonitrile via aza Michael addition and a broad range of modified oligomers have been prepared with CN:NH₂ ratio ranging between 0.1 and 1. NMR and FTnIR analysis reveals that acrylonitrile modification proceeds without formation of tertiary amines. Modified oligomers have been characterized by DSC and analysis of Tg reveals that the adducts are self-associated probably due to weak hydrogen bonding and dipole interactions. The modified oligomers with a modification degree higher than 0.4 were miscible with DGEBA. The low and high temperature relaxations of the cured thermosets have been measured by DMTA. In addition to the commonly observed β₂ relaxation, a new β₁ process linked by an isosbestic point to β₂ has been found. β₁ is attributed to an extended segment comprising the pendant propionitrile group as well as the aminopropyl segment that connects tertiary amines to the polysiloxane backbone. Elastic modulus as well as the α relaxation can be tuned from high Tg and high rubbery modulus to low Tg and high damping thermosets changing the nitrile content. The experimental network structure obtained from elastic measurements and the Tg were related through well established structure-property relations.
Description
Keywords
Epoxy resins, Hybrid thermoset, Polysiloxane
Bibliographic citation
Loayza, A., Cabanelas, J. C., González, M. G. & Baselga, J. (2015). Critical examination of chemically modified hybrid thermosets: Synthesis, characterization and mechanical behavior in the plateau regime of polyaminosiloxane-nitrile-DGEBA. Polymer, 69, pp. 178-185.